Jun‐ichi Matsuo

3.0k total citations
112 papers, 2.3k citations indexed

About

Jun‐ichi Matsuo is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Jun‐ichi Matsuo has authored 112 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Organic Chemistry, 18 papers in Molecular Biology and 12 papers in Inorganic Chemistry. Recurrent topics in Jun‐ichi Matsuo's work include Asymmetric Synthesis and Catalysis (51 papers), Synthetic Organic Chemistry Methods (30 papers) and Synthesis and Catalytic Reactions (29 papers). Jun‐ichi Matsuo is often cited by papers focused on Asymmetric Synthesis and Catalysis (51 papers), Synthetic Organic Chemistry Methods (30 papers) and Synthesis and Catalytic Reactions (29 papers). Jun‐ichi Matsuo collaborates with scholars based in Japan and Czechia. Jun‐ichi Matsuo's co-authors include Hiroyuki Ishibashi, Teruaki Mukaiyama, Masahiro Murakami, Shu̅ Kobayashi, Hideo Kitagawa, Hiroyuki Tanaka, Daisuke Iida, Shun Sasaki, Tomoyuki Yoshimura and Takehiro Tsuchiya and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Jun‐ichi Matsuo

110 papers receiving 2.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jun‐ichi Matsuo Japan 27 2.1k 348 344 132 101 112 2.3k
Hisanori Nambu Japan 29 2.6k 1.2× 324 0.9× 396 1.2× 68 0.5× 100 1.0× 87 2.8k
Kenichi Murai Japan 26 1.7k 0.8× 326 0.9× 670 1.9× 126 1.0× 87 0.9× 93 2.0k
Julian C. Lo United States 5 2.2k 1.1× 241 0.7× 474 1.4× 79 0.6× 77 0.8× 5 2.5k
Kiyoharu Nishide Japan 27 1.7k 0.8× 572 1.6× 304 0.9× 175 1.3× 169 1.7× 103 2.1k
Carla Obradors Spain 14 2.5k 1.2× 219 0.6× 609 1.8× 71 0.5× 73 0.7× 17 2.7k
C. Wade Downey United States 17 1.5k 0.7× 396 1.1× 428 1.2× 57 0.4× 81 0.8× 35 1.7k
Masahiro Egi Japan 28 2.0k 0.9× 447 1.3× 309 0.9× 96 0.7× 74 0.7× 56 2.3k
Yoo Tanabe Japan 32 2.5k 1.2× 740 2.1× 282 0.8× 66 0.5× 140 1.4× 140 2.9k
Yukio Masaki Japan 25 1.8k 0.9× 316 0.9× 362 1.1× 78 0.6× 79 0.8× 137 2.1k
Tuyêt Jeffery France 19 2.1k 1.0× 324 0.9× 257 0.7× 62 0.5× 103 1.0× 22 2.2k

Countries citing papers authored by Jun‐ichi Matsuo

Since Specialization
Citations

This map shows the geographic impact of Jun‐ichi Matsuo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jun‐ichi Matsuo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jun‐ichi Matsuo more than expected).

Fields of papers citing papers by Jun‐ichi Matsuo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jun‐ichi Matsuo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jun‐ichi Matsuo. The network helps show where Jun‐ichi Matsuo may publish in the future.

Co-authorship network of co-authors of Jun‐ichi Matsuo

This figure shows the co-authorship network connecting the top 25 collaborators of Jun‐ichi Matsuo. A scholar is included among the top collaborators of Jun‐ichi Matsuo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jun‐ichi Matsuo. Jun‐ichi Matsuo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hamada, Shohei, et al.. (2025). Strain-promoted azide–alkyne cycloaddition enhanced by secondary interactions. Organic & Biomolecular Chemistry. 23(8). 1837–1840. 2 indexed citations
2.
Yoshimura, Tomoyuki, et al.. (2023). Aldol/Brook/Carbon Skeletal Rearrangement Cascade Reactions of β‐Silyl Ketones with Aldehydes. European Journal of Organic Chemistry. 26(44).
3.
Yoshimura, Tomoyuki, et al.. (2023). Asymmetric Cycloaddition Reactions of Aryne Intermediates with a Chiral Carbon–Carbon Axis: Syntheses of Axially Chiral Biaryl Compounds. Organic Letters. 25(49). 8952–8956. 1 indexed citations
4.
Nakamichi, Noritaka, Tomoyuki Yoshimura, Yusuke Masuo, et al.. (2020). Homostachydrine is a Xenobiotic Substrate of OCTN1/SLC22A4 and Potentially Sensitizes Pentylenetetrazole-Induced Seizures in Mice. Neurochemical Research. 45(11). 2664–2678. 12 indexed citations
5.
Yoshimura, Tomoyuki, et al.. (2020). Development of Nitrolactonization Mediated by Iron(III) Nitrate Nonahydrate. Chemical and Pharmaceutical Bulletin. 68(12). 1220–1225. 4 indexed citations
6.
Matsuo, Jun‐ichi & Masahiro Murakami. (2013). The Mukaiyama Aldol Reaction: 40 Years of Continuous Development. Angewandte Chemie International Edition. 52(35). 9109–9118. 244 indexed citations
7.
Tanaka, Hiroyuki, et al.. (2012). Regioselective Inter‐ and Intramolecular Formal [4+2] Cycloaddition of Cyclobutanones with Indoles and Total Synthesis of (±)‐Aspidospermidine. Angewandte Chemie International Edition. 52(3). 906–910. 149 indexed citations
8.
Matsuo, Jun‐ichi, et al.. (2010). Titanium(IV) Chloride-Mediated Carbon−Carbon Bond-Forming Reaction between 3,3-Dialkylcyclobutanones and Aldehydes. Organic Letters. 12(17). 3960–3962. 7 indexed citations
9.
Shirahata, Tatsuya, et al.. (2010). Improved catalytic and stereoselective glycosylation with glycosyl N-trichloroacetylcarbamate: application to various 1-hydroxy sugars. Carbohydrate Research. 345(6). 740–749. 11 indexed citations
10.
Matsuo, Jun‐ichi, et al.. (2010). Intramolecular formal [4+2] cycloaddition of 3-ethoxycyclobutanones and alkenes. Chemical Communications. 46(6). 934–934. 26 indexed citations
11.
Matsuo, Jun‐ichi, et al.. (2006). A mild and convenient synthesis of N-carbobenzyloxy ketimines. Chemical Communications. 2896–2896. 14 indexed citations
12.
Matsuo, Jun‐ichi, et al.. (2006). Oxidative Mannich Reaction ofN-Carbobenzyloxy Amines with 1,3-Dicarbonyl Compounds. Organic Letters. 8(19). 4371–4374. 23 indexed citations
13.
Matsuo, Jun‐ichi. (2004). New Oxidations Using Sulfinimidoyl Chlorides. Journal of Synthetic Organic Chemistry Japan. 62(6). 574–583. 13 indexed citations
14.
Matsuo, Jun‐ichi, et al.. (2004). One-pot dehydrogenation of carboxylic acid derivatives to α,β-unsaturated carbonyl compounds under mild conditions. Tetrahedron Letters. 46(3). 407–410. 35 indexed citations
15.
Matsuo, Jun‐ichi, et al.. (2003). N-tert-Butylbenzenesulfenamide-catalyzed oxidation of alcohols to the corresponding carbonyl compounds with N-chlorosuccinimide. Tetrahedron. 59(35). 6739–6750. 59 indexed citations
16.
Matsuo, Jun‐ichi, et al.. (2003). A Convenient Method for the Synthesis of β,γ-Unsaturated Amines from Alkenes via α,β-Unsaturated Diphenylsulfonium Salts. Chemistry Letters. 32(7). 626–627. 25 indexed citations
17.
Matsuo, Jun‐ichi, et al.. (2003). A Convenient Method for the Synthesis of 2-Arylaziridines from Styrene Derivatives via 2-Arylethenyl(diphenyl)sulfonium Salts. Chemistry Letters. 32(4). 392–393. 60 indexed citations
18.
Shimamura, Tadashi, et al.. (2000). Aldol Reaction of Enol Esters Catalyzed by Cationic Species Paired with Tetrakis(pentafluorophenyl)borate.. Chemical and Pharmaceutical Bulletin. 48(11). 1838–1840. 32 indexed citations
19.
Mukaiyama, Teruaki, et al.. (2000). Lithium Tetrakis(pentafluorophenyl)borate-Catalyzed Friedel–Crafts Benzylation Reactions. Chemistry Letters. 29(9). 1010–1011. 11 indexed citations
20.
Matsuo, Jun‐ichi, et al.. (1976). Study on the Bonding Strength of the Silicone Lining Material to Methyl Methacrylate. Nihon Hotetsu Shika Gakkai Zasshi. 20(2). 173–178. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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